Evidence map›Paper›PMID 38806270›Full record

ArticleAnnals of family medicine

"We Feel Alone and Not Listened To": Parents' Perspectives on Pediatric Serious Illness Care in Somali, Hmong, and Latin American Communities.

Jennifer Needle, Sey Lee, Amran Ahmed, Rodolfo Batres, Jinhee Cha, Pilar de la Parra, Shannon Pergament, Kathleen A Culhane-Pera

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Article in Annals of family medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Jennifer NeedleUniversity of Minnesota, Minneapolis, Minnesota jneedle@umn.edu.
Sey LeeSoLaHmo Partnership for Health and Wellness, St Paul, Minnesota.
Amran AhmedSoLaHmo Partnership for Health and Wellness, St Paul, Minnesota.
Rodolfo BatresSoLaHmo Partnership for Health and Wellness, St Paul, Minnesota.
Jinhee ChaSoLaHmo Partnership for Health and Wellness, St Paul, Minnesota.
Pilar de la ParraSoLaHmo Partnership for Health and Wellness, St Paul, Minnesota.
Shannon PergamentWest Side Community Health Services, St Paul, Minnesota.
Kathleen A Culhane-PeraUniversity of Minnesota, Minneapolis, Minnesota.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe experience of ethnically diverse parents of children with serious illness in the US health care system has not been well studied. Listening to families from these communities about their experiences could identify modifiable barriers to quality pediatric serious illness care and facilitate the development of potential improvements. Our aim was to explore parents' perspectives of their children's health care for serious illness from Somali, Hmong, and Latin-American communities in Minnesota.

methodsWe conducted a qualitative study with focus groups and individual interviews using immersion-crystallization data analysis with a community-based participatory research approach.

resultsTwenty-six parents of children with serious illness participated (8 Somali, 10 Hmong, and 8 Latin-American). Parents desired 2-way trusting and respectful relationships with medical staff. Three themes supported this trust, based on parents' experiences with challenging and supportive health care: (1) Informed understanding allows parents to understand and be prepared for their child's medical care; (2) Compassionate interactions with staff allow parents to feel their children are cared for; (3) Respected parental advocacy allows parents to feel their wisdom is heard. Effective communication is 1 key to improving understanding, expressing compassion, and partnering with parents, including quality medical interpretation for low-English proficient parents.

conclusionsParents of children with serious illness from Somali, Hmong, and Latin-American communities shared a desire for improved relationships with staff and improved health care processes. Processes that enhance communication, support, and connection, including individual and system-level interventions driven by community voices, hold the potential for reducing health disparities in pediatric serious illness.

Indexed as

Critical IllnessDelivery of Health CareFocus GroupsParentsProfessional-Family RelationsAdolescentAdultAsianChildChild, PreschoolCommunity-Based Participatory ResearchEast African PeopleFemaleHispanic or LatinoHumansInfantcommunicationcommunity-based participatory researchhealth disparitiespediatric health carequalitative research

Identifiers

PMID38806270
PMCPMC11237228

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.